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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 877291Erstellt: 24. Oktober 2026

Ethanol → 4-(7-Phenylbenz[a]anthracen-4-yl)-7-phenylbenz[a]anthracene

https://huagongshe.com/de/reaction/877291

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktPhenylboronic AcidHCID 66827—
EduktN-bromobutanimideHCID 67184—
Edukt4-(Benz[a]anthracen-4-yl)benz[a]anthraceneHCID 59412552—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(7-Phenylbenz[a]anthracen-4-yl)-7-phenylbenz[a]anthraceneHCID 59412710—

Reaktionsschritte

19.6 g (110 mmol) of N-bromosuccinimide are added in one portion at 100° C. with vigorous stirring to a suspension of 22.7 g (50 mmol) of 4-(benz[a]anthracen-4-yl)benz[a]anthracene in 1000 ml of DMF. The suspension is kept at 100° C. for a further 30 min. and cooled, and 1000 ml of ethanol are then added. The precipitated solid is filtered off with suction, washed three times with 100 ml of ethanol each time and dried in vacuo. The resultant solid is reacted analogously to Example 7 with 15.9 g (130 mmol) of benzeneboronic acid, Recrystallisation five times from DMF (about 6 ml/g); sublimation (p=5×10−5 mbar, T=360° C.). Yield: 21.8 g (36 mmol), 72.0%, purity 99.9% (HPLC), Tg=181.4° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08986852B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-52646a4582bf43ba9c9fb5c133992734
Quellennotizuspto-grants-2015_03